Benzyl chloroformate → Benzyl [4-(benzyloxy)-3-fluorophenyl]carbamate

HRID 2279661Notes

Reaction equation

HRID 2279661 reaction equation
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[CH:11][C:10]=1[F:18])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)(O)[O-].[Na+].Cl[C:25]([O:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)=[O:26].CCCCCC.C(OCC)(=O)C>C(OCC)(=O)C.[Pt]>[CH2:28]([O:27][C:25](=[O:26])[NH:15][C:12]1[CH:13]=[CH:14][C:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[C:10]([F:18])[CH:11]=1)[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1

Participants

7

Reactant 4

HCID 10387Benzyl chloroformateHCID 516892Sodium Bicarbonate2×HCID 21226206Ethyl acetate hexaneHCID 220309121-(Benzyloxy)-2-fluoro-4-nitrobenzene

Product 1

HCID 57754845Benzyl [4-(benzyloxy)-3-fluorophenyl]carbamate

Reagents, catalysts & solvents 2

HCID 23939PlatinumCatalystHCID 8857Ethyl AcetateSolvent

Conditions

Temperature
5 °C

Procedure

A solution of 34.9 g 1-benzyloxy-2-fluoro-4-nitro-benzene (WO03064413) (MW: 247.28, 141 mmol) and 340 mg platinum 5% on activated carbon in 350 ml ethyl acetate was stirred under hydrogen at rt, and normal pressure. The reaction was monitored by HPLC and was complete after twenty hours. The catalyst was filtered over a glass fiber filter, and the filtrate evaporated under reduced pressure to dryness. The oily residue was dissolved in 500 ml acetone and treated with 250 ml of a saturated solution of sodium bicarbonate and 17.5 g of sodium bicarbonate (MW: 84.01, 208 mmol). The mixture was cooled to 5° C. and treated drop wise with 26.08 g of benzyl chloroformate (MW: 170.59, 152 mmol). The reaction was allowed to stirred at room temperature for two hours and monitored by TLC (hexane/ethyl acetate 3:1). The acetone was evaporated, the residue diluted with 500 ml water, and the solid filtered off. The crystals were washed with 500 ml water and dried. Yield: 48.05 g, 95.8%. MS: 352.5 (M+H)+, 350.8, (M−H)−. Method ESI+, ESI−.

Workup

  1. waitwas complete after twenty hours
  2. filtrationThe catalyst was filtered over a glass fiber
  3. filtrationfilter
  4. customthe filtrate evaporated under reduced pressure to dryness
  5. dissolutionThe oily residue was dissolved in 500 ml acetone
  6. customThe acetone was evaporated
  7. additionthe residue diluted with 500 ml water
  8. filtrationthe solid filtered off
  9. washThe crystals were washed with 500 ml water
  10. customdried

Sources & evidence

ORD record
ord-acd91779ac644f17837636ece1cfc3e2
Source dataset
uspto-grants-2015_09
Patent number
US09133213B2

Reaction notes

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